'The Medical Devices Introductory Course', London, UK
3 June 2013 - 3 June 2013
United Kingdom
An event entitled 'The Medical Devices Introductory Course' will be held from 3 to 5 June 2013 in London, UK.
Many people now live healthier, more productive and independent lives as a result of the innovations the medical technology industry has developed. This course aims to provide a comprehensive introduction to one of the most rapidly advancing industries through structured modules on medical device regulatory affairs, put together by practising professionals.
The course will provide people new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU with a combination of lectures and interactive case studies designed to apply theory to practice. Further presentation topics include classification of medical devices, audits, conformity assessments and risk management.
Over the three day course participants can expect an intensive insight in to the medical device and in-vitro diagnostics industry and an opportunity to meet, interact with peers and network with a large variety of leading industry and regulatory agency specialists.For further information, please visit:
http://www.topra.org/meddevintro(opens in new window)
Many people now live healthier, more productive and independent lives as a result of the innovations the medical technology industry has developed. This course aims to provide a comprehensive introduction to one of the most rapidly advancing industries through structured modules on medical device regulatory affairs, put together by practising professionals.
The course will provide people new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU with a combination of lectures and interactive case studies designed to apply theory to practice. Further presentation topics include classification of medical devices, audits, conformity assessments and risk management.
Over the three day course participants can expect an intensive insight in to the medical device and in-vitro diagnostics industry and an opportunity to meet, interact with peers and network with a large variety of leading industry and regulatory agency specialists.For further information, please visit:
http://www.topra.org/meddevintro(opens in new window)